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Bilateral adrenal myelolipoma associated with adrenogenital syndrome
Manabu Sakaki1, Hirofumi Izaki, Tomoharu Fukumori
1Department of Urology, The University of Tokushima School of Medicine, Tokushima, Japan.
Abstract:
Adrenal myelolipoma is a rare benign tumor, occasionally reported in association with endocrine disorders. We report herein a case of bilateral adrenal myelolipoma associated with adrenogenital syndrome caused by 21-hydroxylase deficiency. A diagnosis of 21-hydroxylase deficiency was confirmed by mutation analysis of the CYP21 gene. Our case represents only the second case of bilateral adrenal myelolipoma associated with adrenogenital syndrome caused by 21-hydroxylase deficiency.
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